CA1210626A - Elements a grains d'iodure d'argent pour la photographie multichrome - Google Patents

Elements a grains d'iodure d'argent pour la photographie multichrome

Info

Publication number: CA1210626A
Authority: CA; Canada
Prior art keywords: silver; emulsion; grains; tabular; blue
Prior art date: 1982-12-20
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired

Application number

CA000439924A

Other languages

English (en)

Inventor

Gary L. House

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Eastman Kodak Co

Original Assignee

Eastman Kodak Co

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1982-12-20

Filing date

1983-10-28

Publication date

1986-09-02

1983-10-28 Application filed by Eastman Kodak Co filed Critical Eastman Kodak Co

1986-09-02 Application granted granted Critical

1986-09-02 Publication of CA1210626A publication Critical patent/CA1210626A/fr

Status Expired legal-status Critical Current

Links

229910021612 Silver iodide Inorganic materials 0.000 title claims abstract description 184
JKFYKCYQEWQPTM-UHFFFAOYSA-N 2-azaniumyl-2-(4-fluorophenyl)acetate Chemical compound OC(=O)C(N)C1=CC=C(F)C=C1 JKFYKCYQEWQPTM-UHFFFAOYSA-N 0.000 title claims abstract description 151
229940045105 silver iodide Drugs 0.000 title claims abstract description 151
239000000839 emulsion Substances 0.000 claims abstract description 460
229910052709 silver Inorganic materials 0.000 claims abstract description 197
239000004332 silver Substances 0.000 claims abstract description 197
-1 silver halide Chemical class 0.000 claims abstract description 171
230000003595 spectral effect Effects 0.000 claims description 50
ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 claims description 41
229910021607 Silver chloride Inorganic materials 0.000 claims description 35
HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 claims description 35
239000013078 crystal Substances 0.000 claims description 34
GGCZERPQGJTIQP-UHFFFAOYSA-N sodium;9,10-dioxoanthracene-2-sulfonic acid Chemical compound [Na+].C1=CC=C2C(=O)C3=CC(S(=O)(=O)O)=CC=C3C(=O)C2=C1 GGCZERPQGJTIQP-UHFFFAOYSA-N 0.000 claims description 34
230000001235 sensitizing effect Effects 0.000 claims description 30
230000005855 radiation Effects 0.000 claims description 27
230000006872 improvement Effects 0.000 claims description 17
238000010521 absorption reaction Methods 0.000 claims description 16
230000008901 benefit Effects 0.000 abstract description 21
239000010410 layer Substances 0.000 description 331
238000009740 moulding (composite fabrication) Methods 0.000 description 118
239000000975 dye Substances 0.000 description 103
BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 81
238000000034 method Methods 0.000 description 66
XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 60
238000001556 precipitation Methods 0.000 description 55
ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 48
238000006243 chemical reaction Methods 0.000 description 45
239000000243 solution Substances 0.000 description 38
206010070834 Sensitisation Diseases 0.000 description 37
230000008313 sensitization Effects 0.000 description 37
150000004820 halides Chemical class 0.000 description 35
230000008569 process Effects 0.000 description 35
108010010803 Gelatin Proteins 0.000 description 32
229920000159 gelatin Polymers 0.000 description 32
239000008273 gelatin Substances 0.000 description 32
235000019322 gelatine Nutrition 0.000 description 32
235000011852 gelatine desserts Nutrition 0.000 description 32
CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 28
238000011161 development Methods 0.000 description 28
230000018109 developmental process Effects 0.000 description 28
150000002500 ions Chemical class 0.000 description 27
238000000576 coating method Methods 0.000 description 26
230000001965 increasing effect Effects 0.000 description 25
235000019580 granularity Nutrition 0.000 description 24
239000000126 substance Substances 0.000 description 24
238000000151 deposition Methods 0.000 description 22
239000000203 mixture Substances 0.000 description 22
230000008021 deposition Effects 0.000 description 21
239000000463 material Substances 0.000 description 21
NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 21
238000002360 preparation method Methods 0.000 description 21
SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 20
239000011248 coating agent Substances 0.000 description 19
230000002829 reductive effect Effects 0.000 description 18
238000011160 research Methods 0.000 description 18
230000035945 sensitivity Effects 0.000 description 18
238000007792 addition Methods 0.000 description 17
239000003795 chemical substances by application Substances 0.000 description 17
230000015572 biosynthetic process Effects 0.000 description 15
238000005755 formation reaction Methods 0.000 description 15
239000011229 interlayer Substances 0.000 description 15
231100000489 sensitizer Toxicity 0.000 description 15
230000005070 ripening Effects 0.000 description 14
238000001228 spectrum Methods 0.000 description 14
AGOYDEPGAOXOCK-KCBOHYOISA-N clarithromycin Chemical compound O([C@@H]1[C@@H](C)C(=O)O[C@@H]([C@@]([C@H](O)[C@@H](C)C(=O)[C@H](C)C[C@](C)([C@H](O[C@H]2[C@@H]([C@H](C[C@@H](C)O2)N(C)C)O)[C@H]1C)OC)(C)O)CC)[C@H]1C[C@@](C)(OC)[C@@H](O)[C@H](C)O1 AGOYDEPGAOXOCK-KCBOHYOISA-N 0.000 description 13
238000000407 epitaxy Methods 0.000 description 13
238000003384 imaging method Methods 0.000 description 13
XMBWDFGMSWQBCA-UHFFFAOYSA-M iodide Chemical compound [I-] XMBWDFGMSWQBCA-UHFFFAOYSA-M 0.000 description 13
150000003839 salts Chemical class 0.000 description 13
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 11
150000001875 compounds Chemical class 0.000 description 11
230000000694 effects Effects 0.000 description 11
230000006870 function Effects 0.000 description 11
238000012545 processing Methods 0.000 description 10
239000002516 radical scavenger Substances 0.000 description 10
239000012266 salt solution Substances 0.000 description 10
238000012546 transfer Methods 0.000 description 10
125000000217 alkyl group Chemical group 0.000 description 9
239000007864 aqueous solution Substances 0.000 description 9
CBEQRNSPHCCXSH-UHFFFAOYSA-N iodine monobromide Chemical compound IBr CBEQRNSPHCCXSH-UHFFFAOYSA-N 0.000 description 9
230000009467 reduction Effects 0.000 description 9
WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 8
125000003118 aryl group Chemical group 0.000 description 8
238000005345 coagulation Methods 0.000 description 8
230000015271 coagulation Effects 0.000 description 8
229920001577 copolymer Polymers 0.000 description 8
IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 8
230000001976 improved effect Effects 0.000 description 7
150000004694 iodide salts Chemical class 0.000 description 7
235000007715 potassium iodide Nutrition 0.000 description 7
229960004839 potassium iodide Drugs 0.000 description 7
ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 7
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 6
238000001514 detection method Methods 0.000 description 6
238000009826 distribution Methods 0.000 description 6
230000031700 light absorption Effects 0.000 description 6
229910001961 silver nitrate Inorganic materials 0.000 description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
238000000149 argon plasma sintering Methods 0.000 description 5
230000001186 cumulative effect Effects 0.000 description 5
RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 5
MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical compound C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 5
229940006461 iodide ion Drugs 0.000 description 5
230000007246 mechanism Effects 0.000 description 5
125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 description 5
235000020004 porter Nutrition 0.000 description 5
KIWUVOGUEXMXSV-UHFFFAOYSA-N rhodanine Chemical compound O=C1CSC(=S)N1 KIWUVOGUEXMXSV-UHFFFAOYSA-N 0.000 description 5
238000000926 separation method Methods 0.000 description 5
239000010944 silver (metal) Substances 0.000 description 5
159000000000 sodium salts Chemical class 0.000 description 5
238000003756 stirring Methods 0.000 description 5
125000001424 substituent group Chemical group 0.000 description 5
150000003567 thiocyanates Chemical class 0.000 description 5
QYSXJUFSXHHAJI-YRZJJWOYSA-N vitamin D3 Chemical compound C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)CCCC(C)C)=C\C=C1\C[C@@H](O)CCC1=C QYSXJUFSXHHAJI-YRZJJWOYSA-N 0.000 description 5
LHYQAEFVHIZFLR-UHFFFAOYSA-L 4-(4-diazonio-3-methoxyphenyl)-2-methoxybenzenediazonium;dichloride Chemical compound [Cl-].[Cl-].C1=C([N+]#N)C(OC)=CC(C=2C=C(OC)C([N+]#N)=CC=2)=C1 LHYQAEFVHIZFLR-UHFFFAOYSA-L 0.000 description 4
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
241000483002 Euproctis similis Species 0.000 description 4
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 4
ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 description 4
SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 4
SJOOOZPMQAWAOP-UHFFFAOYSA-N [Ag].BrCl Chemical compound [Ag].BrCl SJOOOZPMQAWAOP-UHFFFAOYSA-N 0.000 description 4
125000003277 amino group Chemical group 0.000 description 4
238000013459 approach Methods 0.000 description 4
125000003710 aryl alkyl group Chemical group 0.000 description 4
239000007844 bleaching agent Substances 0.000 description 4
150000003842 bromide salts Chemical class 0.000 description 4
229910052799 carbon Inorganic materials 0.000 description 4
125000004432 carbon atom Chemical group C* 0.000 description 4
239000003054 catalyst Substances 0.000 description 4
239000000084 colloidal system Substances 0.000 description 4
238000007796 conventional method Methods 0.000 description 4
239000011258 core-shell material Substances 0.000 description 4
125000000623 heterocyclic group Chemical group 0.000 description 4
229910052739 hydrogen Inorganic materials 0.000 description 4
239000001257 hydrogen Substances 0.000 description 4
125000004435 hydrogen atom Chemical group [H]* 0.000 description 4
239000003112 inhibitor Substances 0.000 description 4
DZVCFNFOPIZQKX-LTHRDKTGSA-M merocyanine Chemical compound [Na+].O=C1N(CCCC)C(=O)N(CCCC)C(=O)C1=C\C=C\C=C/1N(CCCS([O-])(=O)=O)C2=CC=CC=C2O\1 DZVCFNFOPIZQKX-LTHRDKTGSA-M 0.000 description 4
230000003287 optical effect Effects 0.000 description 4
239000004848 polyfunctional curative Substances 0.000 description 4
239000001103 potassium chloride Substances 0.000 description 4
235000011164 potassium chloride Nutrition 0.000 description 4
150000003378 silver Chemical class 0.000 description 4
229910052708 sodium Inorganic materials 0.000 description 4
239000011734 sodium Substances 0.000 description 4
229920002554 vinyl polymer Polymers 0.000 description 4
IMSODMZESSGVBE-UHFFFAOYSA-N 2-Oxazoline Chemical compound C1CN=CO1 IMSODMZESSGVBE-UHFFFAOYSA-N 0.000 description 3
RKJUIXBNRJVNHR-UHFFFAOYSA-N 3H-indole Chemical compound C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 description 3
SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 3
241000282320 Panthera leo Species 0.000 description 3
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 3
RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
239000002253 acid Substances 0.000 description 3
229910021529 ammonia Inorganic materials 0.000 description 3
IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 3
238000004061 bleaching Methods 0.000 description 3
238000011109 contamination Methods 0.000 description 3
230000001276 controlling effect Effects 0.000 description 3
230000000875 corresponding effect Effects 0.000 description 3
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238000006073 displacement reaction Methods 0.000 description 3
239000012153 distilled water Substances 0.000 description 3
239000012992 electron transfer agent Substances 0.000 description 3
230000001747 exhibiting effect Effects 0.000 description 3
WJRBRSLFGCUECM-UHFFFAOYSA-N hydantoin Chemical compound O=C1CNC(=O)N1 WJRBRSLFGCUECM-UHFFFAOYSA-N 0.000 description 3
229940091173 hydantoin Drugs 0.000 description 3
238000010348 incorporation Methods 0.000 description 3
238000005259 measurement Methods 0.000 description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
238000001000 micrograph Methods 0.000 description 3
230000005012 migration Effects 0.000 description 3
238000013508 migration Methods 0.000 description 3
239000007800 oxidant agent Substances 0.000 description 3
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
229920000642 polymer Polymers 0.000 description 3
239000002243 precursor Substances 0.000 description 3
239000002904 solvent Substances 0.000 description 3
239000003381 stabilizer Substances 0.000 description 3
125000003107 substituted aryl group Chemical group 0.000 description 3
CBDKQYKMCICBOF-UHFFFAOYSA-N thiazoline Chemical compound C1CN=CS1 CBDKQYKMCICBOF-UHFFFAOYSA-N 0.000 description 3
WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 3
229910052721 tungsten Inorganic materials 0.000 description 3
239000010937 tungsten Substances 0.000 description 3
LBUJPTNKIBCYBY-UHFFFAOYSA-N 1,2,3,4-tetrahydroquinoline Chemical compound C1=CC=C2CCCNC2=C1 LBUJPTNKIBCYBY-UHFFFAOYSA-N 0.000 description 2
AIGNCQCMONAWOL-UHFFFAOYSA-N 1,3-benzoselenazole Chemical compound C1=CC=C2[se]C=NC2=C1 AIGNCQCMONAWOL-UHFFFAOYSA-N 0.000 description 2
BCMCBBGGLRIHSE-UHFFFAOYSA-N 1,3-benzoxazole Chemical compound C1=CC=C2OC=NC2=C1 BCMCBBGGLRIHSE-UHFFFAOYSA-N 0.000 description 2
XJDDLMJULQGRLU-UHFFFAOYSA-N 1,3-dioxane-4,6-dione Chemical compound O=C1CC(=O)OCO1 XJDDLMJULQGRLU-UHFFFAOYSA-N 0.000 description 2
UHKAJLSKXBADFT-UHFFFAOYSA-N 1,3-indandione Chemical compound C1=CC=C2C(=O)CC(=O)C2=C1 UHKAJLSKXBADFT-UHFFFAOYSA-N 0.000 description 2
ODIRBFFBCSTPTO-UHFFFAOYSA-N 1,3-selenazole Chemical compound C1=C[se]C=N1 ODIRBFFBCSTPTO-UHFFFAOYSA-N 0.000 description 2
AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 2
ZRHUHDUEXWHZMA-UHFFFAOYSA-N 1,4-dihydropyrazol-5-one Chemical compound O=C1CC=NN1 ZRHUHDUEXWHZMA-UHFFFAOYSA-N 0.000 description 2
KAMCBFNNGGVPPW-UHFFFAOYSA-N 1-(ethenylsulfonylmethoxymethylsulfonyl)ethene Chemical compound C=CS(=O)(=O)COCS(=O)(=O)C=C KAMCBFNNGGVPPW-UHFFFAOYSA-N 0.000 description 2
HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 2
SVTFGFLBXLUFME-UHFFFAOYSA-N 2,5-dihydroxy-4-octadecan-2-ylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCCCCCC(C)C1=CC(O)=C(S(O)(=O)=O)C=C1O SVTFGFLBXLUFME-UHFFFAOYSA-N 0.000 description 2
125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 2
UGWULZWUXSCWPX-UHFFFAOYSA-N 2-sulfanylideneimidazolidin-4-one Chemical compound O=C1CNC(=S)N1 UGWULZWUXSCWPX-UHFFFAOYSA-N 0.000 description 2
MVVFUAACPKXXKJ-UHFFFAOYSA-N 4,5-dihydro-1,3-selenazole Chemical compound C1CN=C[Se]1 MVVFUAACPKXXKJ-UHFFFAOYSA-N 0.000 description 2
INVVMIXYILXINW-UHFFFAOYSA-N 5-methyl-1h-[1,2,4]triazolo[1,5-a]pyrimidin-7-one Chemical compound CC1=CC(=O)N2NC=NC2=N1 INVVMIXYILXINW-UHFFFAOYSA-N 0.000 description 2
241001479434 Agfa Species 0.000 description 2
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
FZERHIULMFGESH-UHFFFAOYSA-N N-phenylacetamide Chemical compound CC(=O)NC1=CC=CC=C1 FZERHIULMFGESH-UHFFFAOYSA-N 0.000 description 2
229910019142 PO4 Inorganic materials 0.000 description 2
GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 2
FOIXSVOLVBLSDH-UHFFFAOYSA-N Silver ion Chemical compound [Ag+] FOIXSVOLVBLSDH-UHFFFAOYSA-N 0.000 description 2
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KXNQKOAQSGJCQU-UHFFFAOYSA-N benzo[e][1,3]benzothiazole Chemical compound C1=CC=C2C(N=CS3)=C3C=CC2=C1 KXNQKOAQSGJCQU-UHFFFAOYSA-N 0.000 description 2
WMUIZUWOEIQJEH-UHFFFAOYSA-N benzo[e][1,3]benzoxazole Chemical compound C1=CC=C2C(N=CO3)=C3C=CC2=C1 WMUIZUWOEIQJEH-UHFFFAOYSA-N 0.000 description 2
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VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 description 2
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229910052741 iridium Inorganic materials 0.000 description 1
GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 1
150000002504 iridium compounds Chemical class 0.000 description 1
125000003253 isopropoxy group Chemical group [H]C([H])([H])C([H])(O*)C([H])([H])[H] 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
AWJUIBRHMBBTKR-UHFFFAOYSA-O isoquinolin-2-ium Chemical compound C1=[NH+]C=CC2=CC=CC=C21 AWJUIBRHMBBTKR-UHFFFAOYSA-O 0.000 description 1
244000145841 kine Species 0.000 description 1
229920000126 latex Polymers 0.000 description 1
238000002386 leaching Methods 0.000 description 1
LFEUVBZXUFMACD-UHFFFAOYSA-H lead(2+);trioxido(oxo)-$l^{5}-arsane Chemical compound [Pb+2].[Pb+2].[Pb+2].[O-][As]([O-])([O-])=O.[O-][As]([O-])([O-])=O LFEUVBZXUFMACD-UHFFFAOYSA-H 0.000 description 1
QDLAGTHXVHQKRE-UHFFFAOYSA-N lichenxanthone Natural products COC1=CC(O)=C2C(=O)C3=C(C)C=C(OC)C=C3OC2=C1 QDLAGTHXVHQKRE-UHFFFAOYSA-N 0.000 description 1
230000000670 limiting effect Effects 0.000 description 1
239000007788 liquid Substances 0.000 description 1
239000000314 lubricant Substances 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
CUONGYYJJVDODC-UHFFFAOYSA-N malononitrile Chemical compound N#CCC#N CUONGYYJJVDODC-UHFFFAOYSA-N 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000006224 matting agent Substances 0.000 description 1
239000012528 membrane Substances 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
125000005641 methacryl group Chemical group 0.000 description 1
229920003145 methacrylic acid copolymer Polymers 0.000 description 1
TWXDDNPPQUTEOV-FVGYRXGTSA-N methamphetamine hydrochloride Chemical compound Cl.CN[C@@H](C)CC1=CC=CC=C1 TWXDDNPPQUTEOV-FVGYRXGTSA-N 0.000 description 1
125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 description 1
239000003607 modifier Substances 0.000 description 1
125000000896 monocarboxylic acid group Chemical group 0.000 description 1
125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 description 1
VMGAPWLDMVPYIA-HIDZBRGKSA-N n'-amino-n-iminomethanimidamide Chemical compound N\N=C\N=N VMGAPWLDMVPYIA-HIDZBRGKSA-N 0.000 description 1
229910017464 nitrogen compound Inorganic materials 0.000 description 1
125000000018 nitroso group Chemical group N(=O)* 0.000 description 1
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000002674 ointment Substances 0.000 description 1
230000003647 oxidation Effects 0.000 description 1
238000007254 oxidation reaction Methods 0.000 description 1
230000036961 partial effect Effects 0.000 description 1
239000002245 particle Substances 0.000 description 1
239000001814 pectin Substances 0.000 description 1
229920001277 pectin Polymers 0.000 description 1
235000010987 pectin Nutrition 0.000 description 1
230000008447 perception Effects 0.000 description 1
230000002093 peripheral effect Effects 0.000 description 1
235000020030 perry Nutrition 0.000 description 1
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
229910052698 phosphorus Inorganic materials 0.000 description 1
239000011574 phosphorus Substances 0.000 description 1
238000005362 photophoresis Methods 0.000 description 1
IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
239000002574 poison Substances 0.000 description 1
231100000614 poison Toxicity 0.000 description 1
229920000233 poly(alkylene oxides) Polymers 0.000 description 1
229920002401 polyacrylamide Polymers 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
229920000768 polyamine Polymers 0.000 description 1
229920001282 polysaccharide Polymers 0.000 description 1
239000005017 polysaccharide Substances 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
229920002717 polyvinylpyridine Polymers 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
150000003142 primary aromatic amines Chemical class 0.000 description 1
230000001737 promoting effect Effects 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical compound O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 description 1
NDGRWYRVNANFNB-UHFFFAOYSA-N pyrazolidin-3-one Chemical compound O=C1CCNN1 NDGRWYRVNANFNB-UHFFFAOYSA-N 0.000 description 1
DNTVKOMHCDKATN-UHFFFAOYSA-N pyrazolidine-3,5-dione Chemical compound O=C1CC(=O)NN1 DNTVKOMHCDKATN-UHFFFAOYSA-N 0.000 description 1
MCSKRVKAXABJLX-UHFFFAOYSA-N pyrazolo[3,4-d]triazole Chemical compound N1=NN=C2N=NC=C21 MCSKRVKAXABJLX-UHFFFAOYSA-N 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
JUJWROOIHBZHMG-UHFFFAOYSA-O pyridinium Chemical compound C1=CC=[NH+]C=C1 JUJWROOIHBZHMG-UHFFFAOYSA-O 0.000 description 1
WVIICGIFSIBFOG-UHFFFAOYSA-N pyrylium Chemical compound C1=CC=[O+]C=C1 WVIICGIFSIBFOG-UHFFFAOYSA-N 0.000 description 1
238000006479 redox reaction Methods 0.000 description 1
BOLDJAUMGUJJKM-LSDHHAIUSA-N renifolin D Natural products CC(=C)[C@@H]1Cc2c(O)c(O)ccc2[C@H]1CC(=O)c3ccc(O)cc3O BOLDJAUMGUJJKM-LSDHHAIUSA-N 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
150000003335 secondary amines Chemical class 0.000 description 1
IMGNYAPMSDUASV-UHFFFAOYSA-K silver arsenate Chemical compound [Ag+].[Ag+].[Ag+].[O-][As]([O-])([O-])=O IMGNYAPMSDUASV-UHFFFAOYSA-K 0.000 description 1
LFAGQMCIGQNPJG-UHFFFAOYSA-N silver cyanide Chemical compound [Ag+].N#[C-] LFAGQMCIGQNPJG-UHFFFAOYSA-N 0.000 description 1
229940098221 silver cyanide Drugs 0.000 description 1
RHUVFRWZKMEWNS-UHFFFAOYSA-M silver thiocyanate Chemical compound [Ag+].[S-]C#N RHUVFRWZKMEWNS-UHFFFAOYSA-M 0.000 description 1
239000002356 single layer Substances 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
241000894007 species Species 0.000 description 1
230000003068 static effect Effects 0.000 description 1
238000007619 statistical method Methods 0.000 description 1
125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
150000003440 styrenes Chemical class 0.000 description 1
125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
125000004964 sulfoalkyl group Chemical group 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
230000000153 supplemental effect Effects 0.000 description 1
230000008093 supporting effect Effects 0.000 description 1
239000000725 suspension Substances 0.000 description 1
239000000979 synthetic dye Substances 0.000 description 1
125000003831 tetrazolyl group Chemical group 0.000 description 1
229910052716 thallium Inorganic materials 0.000 description 1
BKVIYDNLLOSFOA-UHFFFAOYSA-N thallium Chemical compound [Tl] BKVIYDNLLOSFOA-UHFFFAOYSA-N 0.000 description 1
230000008719 thickening Effects 0.000 description 1
150000003568 thioethers Chemical class 0.000 description 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
229910001428 transition metal ion Inorganic materials 0.000 description 1
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
BJAARRARQJZURR-UHFFFAOYSA-N trimethylazanium;hydroxide Chemical compound O.CN(C)C BJAARRARQJZURR-UHFFFAOYSA-N 0.000 description 1
238000000108 ultra-filtration Methods 0.000 description 1
238000009827 uniform distribution Methods 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
230000000007 visual effect Effects 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1
239000011701 zinc Substances 0.000 description 1
229910052984 zinc sulfide Inorganic materials 0.000 description 1

Classifications

- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
- G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
- G03C7/3022—Materials with specific emulsion characteristics, e.g. thickness of the layers, silver content, shape of AgX grains

Landscapes

Physics & Mathematics (AREA)
General Physics & Mathematics (AREA)
Silver Salt Photography Or Processing Solution Therefor (AREA)

CA000439924A 1982-12-20 1983-10-28 Elements a grains d'iodure d'argent pour la photographie multichrome Expired CA1210626A (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US45136682A	1982-12-20	1982-12-20
US451,366		1982-12-20

Publications (1)

Publication Number	Publication Date
CA1210626A true CA1210626A (fr)	1986-09-02

Family

ID=23791907

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA000439924A Expired CA1210626A (fr)	1982-12-20	1983-10-28	Elements a grains d'iodure d'argent pour la photographie multichrome

Country Status (4)

Country	Link
EP (1)	EP0111919B1 (fr)
JP (1)	JPS59119350A (fr)
CA (1)	CA1210626A (fr)
DE (1)	DE3371254D1 (fr)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS6172234A (ja) *	1984-09-14	1986-04-14	Konishiroku Photo Ind Co Ltd	ハロゲン化銀カラ−写真感光材料
JPS6172235A (ja) *	1984-09-14	1986-04-14	Konishiroku Photo Ind Co Ltd	ハロゲン化銀カラ−写真感光材料
JPH0685056B2 (ja) *	1985-07-18	1994-10-26	富士写真フイルム株式会社	カラー写真感光材料
JPH0715571B2 (ja) *	1985-07-19	1995-02-22	富士写真フイルム株式会社	ハロゲン化銀カラ−写真感光材料
JP2655141B2 (ja) *	1985-07-23	1997-09-17	富士写真フイルム株式会社	ハロゲン化銀乳剤の製造方法
JPH0650381B2 (ja) *	1985-08-05	1994-06-29	富士写真フイルム株式会社	ハロゲン化銀カラ−感光材料の処理方法
US4672027A (en) *	1985-10-23	1987-06-09	Eastman Kodak Company	Multicolor photographic element with a minus blue recording tabular grain emulsion layer overlying a blue recording emulsion layer
US4693964A (en) *	1985-10-23	1987-09-15	Eastman Kodak Company	Multicolor photographic element with a tabular grain emulsion layer overlying a minus blue recording emulsion layer
JPS62151840A (ja) *	1985-12-26	1987-07-06	Fuji Photo Film Co Ltd	高アスペクト比のヨウ臭化銀乳剤の調製方法
AU591540B2 (en) *	1985-12-28	1989-12-07	Konishiroku Photo Industry Co., Ltd.	Method of processing light-sensitive silver halide color photographic material
JP2607362B2 (ja) *	1986-01-20	1997-05-07	コニカ株式会社	ハロゲン化銀カラー写真感光材料
JP2619238B2 (ja) *	1986-03-05	1997-06-11	コニカ株式会社	ハロゲン化銀カラー写真感光材料
JP2634059B2 (ja) *	1988-04-08	1997-07-23	富士写真フイルム株式会社	ハロゲン化銀カラー写真感光材料
US5250403A (en) *	1991-04-03	1993-10-05	Eastman Kodak Company	Photographic elements including highly uniform silver bromoiodide tabular grain emulsions
US5476760A (en)	1994-10-26	1995-12-19	Eastman Kodak Company	Photographic emulsions of enhanced sensitivity
US6994952B2 (en)	2002-03-22	2006-02-07	Fuji Photo Film Co., Ltd.	Silver halide emulsion and production process thereof
US7129032B2 (en)	2003-10-24	2006-10-31	Fuji Photo Film Co., Ltd	Black and white photothermographic material and image forming method
CN102636952A (zh) *	2012-04-19	2012-08-15	蔡新民	一种防止激光光绘菲林变形的制作方法
CN109743051A (zh) *	2019-03-22	2019-05-10	广东美的制冷设备有限公司	驱动控制电路和家电设备

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB1507989A (en) *	1974-12-19	1978-04-19	Ciba Geigy Ag	Photographic emulsions
US4184877A (en) *	1976-06-10	1980-01-22	Ciba-Geigy Ag	Process for the manufacture of photographic silver halide emulsions containing silver halide crystals of the twinned type
US4434226A (en) *	1981-11-12	1984-02-28	Eastman Kodak Company	High aspect ratio silver bromoiodide emulsions and processes for their preparation

1983
- 1983-10-28 CA CA000439924A patent/CA1210626A/fr not_active Expired
- 1983-12-19 EP EP19830112771 patent/EP0111919B1/fr not_active Expired
- 1983-12-19 DE DE8383112771T patent/DE3371254D1/de not_active Expired
- 1983-12-20 JP JP23903183A patent/JPS59119350A/ja active Pending

Also Published As

Publication number	Publication date
EP0111919B1 (fr)	1987-04-29
EP0111919A2 (fr)	1984-06-27
EP0111919A3 (en)	1984-10-10
DE3371254D1 (en)	1987-06-04
JPS59119350A (ja)	1984-07-10

Legal Events

Date	Code	Title	Description
2003-10-28	MKEX	Expiry

Publication	Publication Date	Title
CA1175697A (fr)	1984-10-09	Emulsions de bromoiodure d'argent sensibles au rayonnement et a grains tabulaires et comportant une partie centrale a faible teneur en i
US4439520A (en)	1984-03-27	Sensitized high aspect ratio silver halide emulsions and photographic elements
CA1175698A (fr)	1984-10-09	Emulsions de chlorobromure d'argent comprenant des grains tabulaires, et avec du chlorure et du bromure disposes en couches annulaires
CA1175700A (fr)	1984-10-09	Procedes d'obtention d'emulsions de bromoiodure d'argent a allongement eleve
CA1175278A (fr)	1984-10-02	Emulsion d'halogenuse d'argent a grains tabulaires et contenenat un sel d'argent dispose par epitaxie selon une certaine configuration superficielle
CA1175691A (fr)	1984-10-09	Procede de precipitation a double jet pour l'obtention de grains tabulaires de chlorure d'argent a allongement eleve
CA1210625A (fr)	1986-09-02	Sensibilisation epitaxiale controlee en site demulsions a teneur limitee d'iodure d'argent
CA1210624A (fr)	1986-09-02	Emulsions d'halogenure d'argent, et elements photographiques a teneur de grains
CA1175693A (fr)	1984-10-09	Emulsions de chlorure d'argent a allongement eleve et a comportement cristallin modifie
CA1210623A (fr)	1986-09-02	Emulsions d'iodure d'argent en phase gamma, elements qui les renferment, et leur emploi
US4490458A (en)	1984-12-25	Multicolor photographic elements containing silver iodide grains
EP0111919B1 (fr)	1987-04-29	Eléments photographiques multicolores contenant des grains d'iodure d'argent
JPH06347928A (ja)	1994-12-22	本来的に安定な粒子面を持つ中位アスペクト比平板状粒子高塩化物乳剤
EP0219850A2 (fr)	1987-04-29	Eléments photographiques multicolores (I)
US4812390A (en)	1989-03-14	Process and element for obtaining a photographic image
JPH0221572B2 (fr)	1990-05-15
JPH0749551A (ja)	1995-02-21	平板状粒子乳剤による電子印刷方法
US5310635A (en)	1994-05-10	Photographic camera film containing a high chloride tabular grain emulsion with tabular grain {100} major faces
US5672467A (en)	1997-09-30	Higher speed color photographic element and a method for high speed imaging
JP3333518B2 (ja)	2002-10-15	色素画像形成性写真要素
JP3268109B2 (ja)	2002-03-25	低銀カラー写真要素および色素画像生成方法
JPS648324B2 (fr)	1989-02-13